rs32935118 SNP Detail

Summary

• ID
  rs32935118
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr12:99551939 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AAGCCATACC TGAACCTCAG
  AAGAAGACAC CTAACTCTGT GGTGGCATTG TCCCTAATGA CCTGTCATCT AACCACCCAG
  TGTGAGCATC AGAGGACTAA CAGGTGCCAA GAGCTTCGGC TCAGCTTAGT CTTCGGTATT
  GACCGGGTCT ACTGGAACTG CTGTTTATTC TTCAACACCG CAGCCTCCAC AGTTCTCCAC
  Y
  TCACTTCTGC AACTTGACCA GTCCTGAGGC TCAAACCTGT GACCTGATAA CGTGAGTCTG
  CAGCAGCACT CTCAGCTGAC GCCTACGGGG ATTTCCCTGG GGTGCACGCA TGCACCCAAA
  CGTGCATTTG CAGCCTAGTG GGAACATTGT GTGTCTTTCT CTATTGATCT CCACCTTGTT
  CCTCTGAGAC AGGGTCTCTC                                            
  
  Y = C/T
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	A/J	MOLF/EiJ	PWD/PhJ
ss47234282	NES11413556	PERLEGEN	MM_PANEL2	f	SNP	T	C	C
SNP Consensus Information
SNP					Consensus Type	A/J	MOLF/EiJ	PWD/PhJ
rs32935118					SNP	T	C	C

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss47234282	NES11413556	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr12:99551939 () rs orientation: forward

Symbol	Name	Function Class
Gm26839	predicted gene, 26839	within coordinates
Gm53755	predicted gene, 53755	within coordinates
Rr269924	regulatory region 269924	1586 bp proximal